
Thermo Fisher Scientific MEK1 Polyclonal Antibody
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Applications
Tested Dilution
Publications
Western Blot (WB)
1 µg/mL
View 1 publication 1 publication
Immunohistochemistry (Paraffin) (IHC (P))
1:20
Immunocytochemistry (ICC/IF)
5 µg/mL
Product Specifications
Published species
Not Applicable
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
A synthetic peptide derived from the N-terminus of human Mek1 protein if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
MEK1,
uniProtId:
Q02750-1,
ncbiNodeId:
9606,
antigenRange:
1,
antigenLength:
393,
antigenImageFileName:
PA5-16556_MEK1_Q02750-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-16556_MEK1_Q02750-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Storage conditions
4° C
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_10983180
Product Specific Information
PA5-16556 targets MEK-1 in WB applications and shows reactivity with mouse, Rat, Xn, and Human samples.
The PA5-16556 immunogen is a synthetic peptide derived from the N-terminus of human Mek1 protein.
Target Information
MAP2K1 (MEK1) kinase is a dual-specificity protein kinase that functions in mitogen-activated protein kinase (MAPK) cascades, controlling cell growth and differentiation. MAP2K1 is activated by a wide variety of growth factors and cytokines and also by membrane-dependent depolarization and calcium influx. Mek1 is activated by phosphorylation of serine 218 and 222 residues by Raf1. It is known to be involved in the signaling during stress activate response, apoptosis and proliferative induction by cytokines. Mutations in the gene can lead to cardiofaciocutaneous syndrome.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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